Human cerebral evolution and the clinical syndrome of amyotrophic lateral sclerosis

Journal of Neurology, Neurosurgery & Psychiatry

Fecha de publicación: 11 April 2019


Autores: Robert D Henderson, Fleur C Garton, Matthew C Kiernan, Martin R Turner, Andrew Eisen.

Background: The adult neurodegenerative disorder amyotrophic lateral sclerosis (ALS) is unmistakeable from clinical descriptions now more than a century old. Neither the site of symptom onset in ALS nor pattern of symptom spread is truly random.

Seguir leyendo

Enviar comentario